Suppliers / Mehta Api

Mehta Api

India 152 employees Updated 9 July 2026

Mehta Api is an API manufacturer based in India. It holds 8 active US drug master files and 2 valid CEPs across a filed portfolio of 10 molecules. Its GMP standing is certified by EMA. Customs aggregates show $5.1M of exports covering 120 molecules to 28 destinations in 2025.

8
active US DMFs
2
valid CEPs
2
registered plants
1
filings across 1 regulators
These figures were checked against the regulators' own files on 25 July 2026
EU GMP
1 of 1 confirmed
Sources: EudraGMDP (MIA + third-country GMP certs), read 4 May 2026.

Registered plants

Site FDA FEI
Boisar, India Not on file
Boisar, India Not on file

What they file, and where

Molecule Regulators Docs
Agomelatine US FDA 1
Bisoprolol EDQM 1
Cariprazine US FDA 1
Cinacalcet US FDA 1
Droperidol US FDA 1
Esmolol US FDA 1
Landiolol US FDA 1
Mirabegron US FDA 1
Rivaroxaban EDQM 1
Vismodegib US FDA 1

Also appears on these molecule pages

Filings and GMP by regulator

Regulator Filings GMP certificates
CDSCO (India) 1 None
EMA None 2

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $453K 13
2025 Not reported $5.1M 28
2024 Not reported $3.0M 23
2023 Not reported $4.1M 32

Export figures are customs aggregates. We do not publish the identity of any buyer.

Questions about Mehta Api

Does Mehta Api hold a US DMF or a CEP?
Mehta Api holds 8 active US drug master files and 2 valid CEPs. A drug master file is a submission to the FDA describing how an ingredient is made; a CEP is the EDQM's certificate that the substance meets its European Pharmacopoeia monograph. Both are filings rather than approvals.
Where does Mehta Api manufacture?
2 registered sites are on record, in India (Boisar among others). Every site is listed on this page with the register it came from.
What does Mehta Api make?
10 molecules are on record against Mehta Api, including Agomelatine, Bisoprolol, Cariprazine and Cinacalcet. Each links through to that molecule's full manufacturer list.
Which regulators recognise Mehta Api's GMP?
Current GMP certificates are on record from EMA. GMP recognition covers the manufacturing site, separately from any filing on the substance itself.

Answered from this company's own record. Where a register holds nothing, the question is not asked rather than answered with a zero. How we count our figures.

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Sources on this page

FDA
Drug master files, establishment registration, inspection classifications
EDQM
Certificates of suitability
EudraGMDP and national regulators
GMP certificates
Customs aggregates
Export values, molecule and destination counts